A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3348273



Internal ID15195255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97566271..97566285hg38UCSC Ensembl
Innerchr10:97566273..97566283hg38UCSC Ensembl
Outerchr10:97566269..97566287hg38UCSC Ensembl
chr10:99326028..99326042hg19UCSC Ensembl
Innerchr10:99326030..99326040hg19UCSC Ensembl
Outerchr10:99326026..99326044hg19UCSC Ensembl
chr10:99316018..99316032hg18UCSC Ensembl
Innerchr10:99316020..99316030hg18UCSC Ensembl
Outerchr10:99316016..99316034hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3850
hg1950
hg1850
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7865411
SamplesNA12005
Known GenesUBTD1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3348273
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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